A citation-based method for searching scientific literature

Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
Times Cited: 70







List of co-cited articles
305 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
138
40

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
229
28


Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
155
22






Research with stored biological samples: what do research participants want?
Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch Intern Med 2005
81
18



Ethics and biobanks.
M G Hansson. Br J Cancer 2009
105
17


Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
125
14


Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
114
14

High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience.
Thomas Malone, Paul J Catalano, Peter J O'Dwyer, Bruce Giantonio. J Natl Cancer Inst 2002
57
15



An empirical survey on biobanking of human genetic material and data in six EU countries.
Isabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, Jenny Duchier, Brigitte Jansen, Jürgen Simon, Paula Lobato De Faria, Anna Perez-Lezaun, Bert Visser, Garrath D Williams,[...]. Eur J Hum Genet 2003
69
13


Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
134
11

Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
55
14

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
184
11

Research on stored biological samples: views of African American and White American cancer patients.
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
66
12

Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
171
11

Informed consent and biobanks.
Ellen Wright Clayton. J Law Med Ethics 2005
58
12





Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
98
8


Biobanking: international norms.
Bartha Maria Knoppers. J Law Med Ethics 2005
63
9

DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
69
8



Banking together. A unified model of informed consent for biobanking.
Elena Salvaterra, Lucilla Lecchi, Silvia Giovanelli, Barbara Butti, Maria Teresa Bardella, Pier Alberto Bertazzi, Silvano Bosari, Guido Coggi, Domenico A Coviello, Faustina Lalatta,[...]. EMBO Rep 2008
61
9

Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.
Linus Johnsson, Mats G Hansson, Stefan Eriksson, Gert Helgesson. BMJ 2008
44
13

Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
105
8

Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
49
12


Ownership and uses of human tissue: does the Nuffield bioethics report accord with opinion of surgical inpatients?
R D Start, W Brown, R J Bryant, M W Reed, S S Cross, G Kent, J C Underwood. BMJ 1996
25
20

Bio-libraries and DNA storage: assessment of patient perception of information.
G Moutel, S de Montgolfier, J P Meningaud, C Hervé. Med Law 2001
14
35

Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
55
9

Tackling community concerns about commercialisation and genetic research: a modest interdisciplinary proposal.
Gillian Haddow, Graeme Laurie, Sarah Cunningham-Burley, Kathryn G Hunter. Soc Sci Med 2007
55
9

The consent problem within DNA biobanks.
Darren Shickle. Stud Hist Philos Biol Biomed Sci 2006
39
12

Informed consent in biobank research: a deliberative approach to the debate.
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
83
7

Why might people donate tissue for cancer research? Insights from organ/tissue/blood donation and clinical research.
Renata E Axler, Rob Irvine, Wendy Lipworth, Bronwen Morrell, Ian H Kerridge. Pathobiology 2008
21
23


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.